Canonical Allele Identifier: CA2689809458

Gene: GALT

Linked Data

• gnomAD v4: 9-34648729-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.34648729C>A , CM000671.2:g.34648729C>A	GRCh38
NC_000009.11:g.34648726C>A , CM000671.1:g.34648726C>A	GRCh37
NC_000009.10:g.34638726C>A	NCBI36
NG_009029.1:g.7092C>A
NG_028966.1:g.1545C>A
NG_009029.2:g.7141C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000691183.1:c.*276-33C>A	ENSP00000509954.1:n.*276-33C>A
ENST00000378842.8:c.688-33C>A MANE Select	ENSP00000368119.4:n.688-33C>A
ENST00000378842.7:c.688-33C>A	ENSP00000368119.3:n.688-33C>A
ENST00000450095.6:c.361-33C>A	ENSP00000401956.2:n.361-33C>A
ENST00000473506.6:c.*276-33C>A	ENSP00000432839.2:n.*276-33C>A
ENST00000473529.5:n.847-33C>A
ENST00000487381.5:n.1345C>A
ENST00000489643.6:n.735C>A
ENST00000554085.5:c.*432-33C>A	ENSP00000450419.1:n.*432-33C>A
ENST00000554550.5:c.*308-33C>A	ENSP00000451435.1:n.*308-33C>A
ENST00000554638.5:n.1160-33C>A
ENST00000555020.5:n.1116C>A
ENST00000555086.5:n.692-33C>A
ENST00000555754.1:n.33-33C>A
ENST00000556244.1:c.675-33C>A
ENST00000556278.1:c.432+273C>A	ENSP00000451792.1:n.432+273C>A
ENST00000557706.5:n.1250-33C>A
NM_000155.3:c.688-33C>A	NP_000146.2:n.688-33C>A
NM_001258332.1:c.361-33C>A	NP_001245261.1:n.361-33C>A
NM_000155.4:c.688-33C>A MANE Select	NP_000146.2:n.688-33C>A
NM_001258332.2:c.361-33C>A	NP_001245261.1:n.361-33C>A